A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18279372



Internal ID20846412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:104913798..104914520hg38UCSC Ensembl
chr9:107676079..107676801hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38723
hg19723
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6565843
Supporting Variants
Samples
Known GenesABCA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18279372
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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